NDC 69313-636 Lidoflex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69313 - Naimco, Inc. Dba Richmar, Inc.
- 69313-636 - Lidoflex
Product Packages
NDC Code 69313-636-01
Package Description: 25.3 mg in 1 POUCH
NDC Code 69313-636-05
Package Description: 25.3 mg in 1 BAG
NDC Code 69313-636-20
Package Description: 25.3 mg in 1 PACKAGE
Product Details
What is NDC 69313-636?
What are the uses for Lidoflex?
Which are Lidoflex UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Lidoflex Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CROSPOVIDONE (UNII: 68401960MK)
- 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".